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Items: 1 to 20 of 317

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7097006copy number variation1nstd102humanUncertain significance GRCh37 chr4: 8,869,419-10,118,290 , GRCh38.p12 chr4: 8,867,693-10,116,666 RNA5SP153, USP17L29, 59 more genes
    nsv7055114inversion1nstd229human GRCh38 chr4: 8,400,925-10,237,375 , GRCh37.p13 chr4: 8,402,652-10,238,999 LOC101928948, SLC2A9-AS1, 65 more genes
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7040714inversion1nstd229human GRCh38 chr4: 8,676,530-9,855,545 , GRCh37.p13 chr4: 8,678,256-9,857,169 LOC101928948, UNC93B8, 56 more genes
    nsv7040058inversion1nstd229human GRCh38 chr4: 9,508,787-9,888,528 , GRCh37.p13 chr4: 9,510,436-9,890,152 DRD5, SNRPCP13, 12 more genes
    nsv6737698copy number variation1nstd229human GRCh38 chr4: 9,532,627-9,973,090 , GRCh37.p13 chr4: 9,534,246-9,974,714 LOC101928948, MIR548I2, 11 more genes
    nsv6737662copy number variation1nstd229human GRCh38 chr4: 9,679,933-10,189,883 , GRCh37.p13 chr4: 9,681,557-10,191,507 ALG1L3P, SLC2A9-AS1, 9 more genes
    nsv6736202copy number variation1nstd229human GRCh38 chr4: 9,649,300-10,719,450 , GRCh37.p13 chr4: 9,650,924-10,721,074 SLC2A9-AS1, LOC100129344, 23 more genes
    nsv6731118copy number variation1nstd229human GRCh38 chr4: 9,646,853-9,768,199 , GRCh37.p13 chr4: 9,648,477-9,769,823 EVA1CP1, FAM86MP, 3 more genes
    nsv6730234copy number variation1nstd229human GRCh38 chr4: 9,753,080-9,763,637 , GRCh37.p13 chr4: 9,754,704-9,765,261 OR7E35P
    nsv6727657copy number variation1nstd229human GRCh38 chr4: 9,726,501-9,767,100 , GRCh37.p13 chr4: 9,728,125-9,768,724 EVA1CP1, OR7E35P
    nsv6726052copy number variation1nstd229human GRCh38 chr4: 9,748,525-9,756,583 , GRCh37.p13 chr4: 9,750,149-9,758,207 OR7E35P
    nsv6723208copy number variation1nstd229human GRCh38 chr4: 5,355,032-14,502,279 , GRCh37.p13 chr4: 5,356,759-14,503,903 OR7E86P, LINC02447, 164 more genes
    nsv6723107copy number variation1nstd229human GRCh38 chr4: 9,680,613-10,868,191 , GRCh37.p13 chr4: 9,682,237-10,869,815 LINC02498, LOC105374479, 24 more genes
    nsv6719506copy number variation1nstd229human GRCh38 chr4: 9,575,444-10,681,382 , GRCh37.p13 chr4: 9,577,068-10,683,006 LOC100287951, LOC105374480, 24 more genes
    nsv6637010copy number variation1nstd102humanUncertain significance GRCh37 chr4: 9,577,433-10,148,655 , GRCh38.p12 chr4: 9,575,809-10,147,031 RNA5SP154, SNRPCP13, 11 more genes
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